Good overview of regulations Medical Devices in Europe - Interactive course

The most important objective achieved for me was to learn more about an assertive approach (problem solving, the I-message,

This course is hands-on and useful for use in work activities on site - I do what I can and I have the means to upgrade my knowledge and support the effectiveness and mostly the reliability of the clinical trial processes and data.

This course gives you a complete overview on different roles in the clinical research

This course gives you the highlights of GCP and is a great starting base for someone who doesn't have previous experience. The trainer thoroughly explained the course material. The workshops were a great way of understanding the theory. And the trainer answered all the questions in a very comprehensive manner.

This course offered me a very good overview of CPM job - The course was really great, and the hand-out is as well highly appreciated. Examples and workshops were perfect, thanks to the qualified and nice trainer. Will definitively recommend it! 

This course gave a very good overview, tips and tricks of being a CPM - different aspects have been combined to a picture and the Job as a CPM does not look that "unsorted" anymore. Before, I would have been afraid to miss or forget important aspects.

It was a very complete course full of good tips and tricks. As I'm new in the job, I did not really know what to expect but I realised that I already do a lot of what Marleen covered. But thanks to Marleen, all the pieces of the puzzle fell into place. Moreover, the course was

This training gave me clarity on successful training methodology, increased my confidence, and provided lots of ideas on keeping classroom lively and enjoyable, effective venue. I enjoyed the energy of the trainer, sharing ideas, practising, giving talk on a potential distractive attendee. I would highly recommend this course as it provides good balance of theory of

It gives an idea why and how risk management is necessary not only in theory but with realistic examples/ discussions. I realised that we do it already, but not naming it risk management. Now we need to start doing it on paper for documentation purposes, within the whole CTT and on a whole clinical trial level.